Doyle T P, Loyd J E, Robbins I M
Division of Pediatric Cardiology and Center for Lung Research, Department of Medicine, Vanderbilt University School of Medicine, Nashville, Tennessee 37232, USA.
Am J Respir Crit Care Med. 2001 Aug 15;164(4):657-60. doi: 10.1164/ajrccm.164.4.2012132.
Mediastinal fibrosis is a rare consequence of infection with the fungus Histoplasma capsulatum that can lead to occlusion of large pulmonary arteries and veins and mainstem bronchi. Medical and surgical treatments for this disorder have been ineffective. We describe successful treatment for central pulmonary arterial and venous obstruction due to mediastinal fibrosis in four patients using percutaneously placed intravascular stents. Patients were severely limited, World Health Organization functional class III or IV. At the time of right and left heart catheterization, stents were placed in pulmonary arteries (n = 1), veins (n = 2), or both (n = 1) to relieve vascular obstruction resulting from mediastinal fibrosis. Immediate hemodynamic and clinical improvement was observed in all patients. Three of the four patients have had sustained improvement in exercise tolerance, from 3.5 mo to 4.5 yr after stent placement. The only complication was a self-limited pulmonary hemorrhage in one patient. Our initial experience suggests that percutaneous stent placement to relieve central pulmonary arterial or venous obstruction due to mediastinal fibrosis is an effective new treatment modality.
纵隔纤维化是荚膜组织胞浆菌感染的一种罕见后果,可导致大型肺动脉、肺静脉和主支气管阻塞。针对这种疾病的药物和手术治疗均无效。我们描述了使用经皮放置血管内支架成功治疗4例因纵隔纤维化导致的中央肺动脉和静脉阻塞的患者。患者病情严重受限,世界卫生组织功能分级为III级或IV级。在左右心导管检查时,在肺动脉(n = 1)、静脉(n = 2)或两者(n = 1)中放置支架,以缓解纵隔纤维化导致的血管阻塞。所有患者均立即出现血流动力学和临床改善。4例患者中有3例运动耐量持续改善,自支架置入后3.5个月至4.5年。唯一的并发症是1例患者出现自限性肺出血。我们的初步经验表明,经皮放置支架以缓解因纵隔纤维化导致的中央肺动脉或静脉阻塞是一种有效的新治疗方式。